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Pharmaceutical Research|May 17, 2008
The quantitative prediction of CYP-mediated drug interaction by physiologically based pharmacokinetic modelingMotohiro Kato, Yoshihisa Shitara, Hitoshi Sato, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 20, 2005
Identification of the hepatic efflux transporters of organic anions using double-transfected Madin-Darby canine kidney II cells expressing human organic anion-transporting polypeptide 1B1 (OATP1B1)/multidrug resistance-associated protein 2, OATP1B1/multidrug resistance 1, and OATP1B1/breast cancer resistance proteinSoichiro Matsushima, Kazuya Maeda, Chihiro Kondo, et al.
Clinical and Translational Science|January 6, 2026
Reimagining Early-Phase Clinical Development in Japan: From Regulatory Obligation to Global AccelerationYasunori Kawakita, Kayoko Matsumoto, Masaru Hirano, et al.
Clinical Pharmacokinetics|January 31, 2015
Effect of Hepatic Impairment on the Pharmacokinetics of Pradigastat, a Diacylglycerol Acyltransferase 1 (DGAT1) InhibitorMasaru Hirano, Dan Meyers, GangaRaju Golla, et al.
Clinical Pharmacology and Therapeutics|May 9, 2006
Effects of organic anion transporting polypeptide 1B1 haplotype on pharmacokinetics of pravastatin, valsartan, and temocaprilKazuya Maeda, Ichiro Ieiri, Kuninobu Yasuda, et al.
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